Cardiac abnormalities in patients with mitochondrial DNA mutation 3243A>G. - Wikidata - awgldk - TriplyDB

Cardiac abnormalities in patients with mitochondrial DNA mutation 3243A>G.

Cardiac abnormalities in patients with mitochondrial DNA mutation 3243A>G.

http://www.wikidata.org/entity/Q24799134

about

Is 2D speckle tracking echocardiography useful for detecting and monitoring myocardial dysfunction in adult m.3243A>G carriers? - a retrospective pilot study Cardiac involvement in mitochondrial DNA disease: clinical spectrum, diagnosis, and management.A family with diabetes and heart failure.Characteristic cardiac phenotypes are detected by cardiovascular magnetic resonance in patients with different clinical phenotypes and genotypes of mitochondrial myopathy.Cardiomyopathy is common in patients with the mitochondrial DNA m.3243A>G mutation and correlates with mutation load.Selection against pathogenic mtDNA mutations in a stem cell population leads to the loss of the 3243A-->G mutation in blood Genetics of dilated cardiomyopathy.Concentric hypertrophic remodelling and subendocardial dysfunction in mitochondrial DNA point mutation carriers.Clinical features, diagnosis and management of maternally inherited diabetes and deafness (MIDD) associated with the 3243A>G mitochondrial point mutation.Clinical and Molecular Characteristics in 100 Chinese Pediatric Patients with m.3243A>G Mutation in Mitochondrial DNA Sudden adult death syndrome in m.3243A>G-related mitochondrial disease: an unrecognized clinical entity in young, asymptomatic adults Defining cardiac adaptations and safety of endurance training in patients with m.3243A>G-related mitochondrial disease.Mitochondrial Heteroplasmy.Inherited Structural Heart Diseases With Potential Atrial Fibrillation Occurrence.MELAS syndrome and cardiomyopathy: linking mitochondrial function to heart failure pathogenesis.Mitochondrial disease and endocrine dysfunction.Quantitative assessment of heteroplasmy of mitochondrial genome: perspectives in diagnostics and methodological pitfalls.Two novel mutations in the beta-myosin heavy chain gene associated with dilated cardiomyopathy.Myocardial glucose uptake in patients with the m.3243A > G mutation in mitochondrial DNA.Monogenic Causes of Diabetes

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Cardiac abnormalities in patients with mitochondrial DNA mutation 3243A>G.

http://www.wikidata.org/entity/Q24799134

description

2002 nî lūn-bûn

@nan

2002 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2002 թվականի օգոստոսին հրատարակված գիտական հոդված

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2002年の論文

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2002年論文

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2002年論文

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2002年論文

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2002年論文

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2002年論文

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2002年论文

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name

Cardiac abnormalities in patients with mitochondrial DNA mutation 3243A>G

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Cardiac abnormalities in patients with mitochondrial DNA mutation 3243A>G.

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Cardiac abnormalities in patients with mitochondrial DNA mutation 3243A>G.

@en

type

label

Cardiac abnormalities in patients with mitochondrial DNA mutation 3243A>G

@nl

Cardiac abnormalities in patients with mitochondrial DNA mutation 3243A>G.

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Cardiac abnormalities in patients with mitochondrial DNA mutation 3243A>G.

@en

prefLabel

Cardiac abnormalities in patients with mitochondrial DNA mutation 3243A>G

@nl

Cardiac abnormalities in patients with mitochondrial DNA mutation 3243A>G.

@ast

Cardiac abnormalities in patients with mitochondrial DNA mutation 3243A>G.

@en

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BMC Cardiovascular Disorders

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Cardiac abnormalities in patients with mitochondrial DNA mutation 3243A>G.

@en

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Ilmo E Hassinen

http://www.w3.org/2001/XMLSchema#string

Kari Majamaa

http://www.w3.org/2001/XMLSchema#string

Keijo Peuhkurinen

http://www.w3.org/2001/XMLSchema#string

Kirsi Majamaa-Voltti

http://www.w3.org/2001/XMLSchema#string

Marja-Leena Kortelainen

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P2860

Sequence and organization of the human mitochondrial genome

Melas: an original case and clinical criteria for diagnosis

Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: a distinctive clinical syndrome

Dilated cardiomyopathy and neonatal lethality in mutant mice lacking manganese superoxide dismutase

Prognostic implications of echocardiographically determined left ventricular mass in the Framingham Heart Study

Cardiomyopathy in the Kearns-Sayre syndrome.

Cardiac involvement in mitochondrial diseases. A study on 17 patients with documented mitochondrial DNA defects.

Mitochondrial DNA mutations in the pathogenesis of human disease.

The emerging concept of mitochondrial cardiomyopathies.

Epidemiology of A3243G, the mutation for mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes: prevalence of the mutation in an adult population.

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10.1186/1471-2261-2-12

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2

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2002-08-01T00:00:00Z

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1046905606

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mitochondrial DNA

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119851

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